Ehlers-Danlos syndrome
The Ehlers–Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
Exact Synonyms
Danlos Disease, Ehlers
Danlos disease
danlos ehlers syndrome
Disease, Ehlers Danlos
Disease, Ehlers-Danlos
Dystrophia mesodermalis congenita
EDS
Ehler Danlos Syndrome
Ehlers Danlos Disease
Ehlers Danlos Syndrome
Ehlers Danlos syndrome
Ehlers-Danlos Disease
Ehlers-Danlos syndromes
elastic skin
Fibrodysplasia elastica generalisata
Hereditary collagen dysplasia
Meekeren-Ehlers-Danlos syndrome
skin elastic
Syndrome, Ehlers-Danlos
Related Synonyms
ED syndrome
class Information
has close match
has exact match
- http://identifiers.org/medgen/41720
- http://identifiers.org/snomedct/398114001
- http://identifiers.org/mesh/D004535
- http://linkedlifedata.com/resource/umls/id/C0013720
- http://purl.bioontology.org/ontology/ICD10CM/Q79.6
- http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1122707206
- Ehlers-Danlos Syndromencit
- Ehlers-Danlos syndromedoid
- Ehlers-Danlos syndromeordo
- https://omim.org/phenotypicSeries/PS130000
has_dbxref
- Ehlers-Danlos syndromedoid
- GARD:6322
- ICD10CM:Q79.6
- icd11.foundation:1122707206
- ICD9:756.83
- MedDRA:10014316
- MEDGEN:41720
- MESH:D004535
- NANDO:1200645
- NANDO:2200607
- Ehlers-Danlos Syndromencit
- NORD:1080
- OMIMPS:130000
- Orphanet:98249
- SCTID:398114001
- UMLS:C0013720
term tracker item